Canonical Allele Identifier: CA793384468
Gene: LINC02357 HGNC NCBI

Linked Data

dbSNP Id: rs1390845259
gnomAD v3: 4-26084009-T-G
gnomAD v4: 4-26084009-T-G
MyVariant Identifiers: chr4:g.26085631T>G (hg19) chr4:g.26084009T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26084009T>G , CM000666.2:g.26084009T>G GRCh38
NC_000004.11:g.26085631T>G , CM000666.1:g.26085631T>G GRCh37
NC_000004.10:g.25694729T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925506.1:n.1401+3419T>G
XR_925506.3:n.1408+3419T>G
Search 100 bp 5'
Search 100 bp 3'